Canonical Allele Identifier: CA1240248745

Gene: SNX17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27375534A= , CM000664.2:g.27375534A=	GRCh38
NC_000002.11:g.27598401A= , CM000664.1:g.27598401A=	GRCh37
NC_000002.10:g.27451905A=	NCBI36
NG_028219.1:g.10211T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233575.7:c.803A= MANE Select	ENSP00000233575.2:p.His268=
ENST00000233575.6:c.803A=	ENSP00000233575.2:p.His268=
ENST00000427123.5:c.*613A=	ENSP00000405399.1:n.*613A=
ENST00000440760.5:c.*648A=	ENSP00000399727.1:n.*648A=
ENST00000453453.1:c.*330A=	ENSP00000401922.1:n.*330A=
ENST00000493711.1:n.520A=
ENST00000537606.5:c.728A=	ENSP00000439208.1:p.His243=
NM_001267059.1:c.767A=	NP_001253988.1:p.His256=
NM_001267060.1:c.728A=	NP_001253989.1:p.His243=
NM_001267061.1:c.743A=	NP_001253990.1:p.His248=
NM_014748.3:c.803A=	NP_055563.1:p.His268=
NR_049782.1:n.1176A=
NR_049783.1:n.1149A=
NR_049784.1:n.1125A=
NR_049785.1:n.1058A=
NR_049786.1:n.1007A=
NR_049787.1:n.858A=
NR_049788.1:n.788A=
XM_011533203.1:c.161A=	XP_011531505.1:p.His54=
XM_011533203.2:c.161A=	XP_011531505.1:p.His54=
XM_017005405.2:c.161A=	XP_016860894.1:p.His54=
NM_014748.4:c.803A= MANE Select	NP_055563.1:p.His268=
NM_001267059.2:c.767A=	NP_001253988.1:p.His256=
NM_001267061.2:c.743A=	NP_001253990.1:p.His248=
NR_049782.2:n.1056A=
NR_049783.2:n.1029A=
NR_049784.2:n.1005A=
NR_049785.2:n.938A=
NR_049786.2:n.887A=
NR_049787.2:n.738A=
NR_049788.2:n.668A=
NM_001267060.2:c.728A=	NP_001253989.1:p.His243=